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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875272copy number variation1nstd102humanLikely benign GRCh37 chr2: 189,298,315-189,468,360 , GRCh38.p12 chr2: 188,433,588-188,603,633 GULP1
    nsv3906919copy number variation1nstd102humanBenign GRCh37 chr2: 189,200,405-189,368,467 , GRCh38 chr2: 188,335,678-188,503,740 , NCBI36 chr2: 188,908,650-189,076,712 GULP1
    nsv3893453copy number variation1nstd102humanBenign GRCh37 chr2: 189,354,436-189,462,552 , NCBI36 chr2: 189,062,681-189,170,797 , GRCh38 chr2: 188,489,709-188,597,825 GULP1
    nsv3897124copy number variation1nstd102humanBenign GRCh37 chr2: 189,248,503-189,354,495 , NCBI36 chr2: 188,956,748-189,062,740 , GRCh38 chr2: 188,383,776-188,489,768 GULP1
    nsv4453943copy number variation1nstd102humanUncertain significance GRCh37 chr2: 189,396,004-189,439,600 , GRCh38.p12 chr2: 188,531,277-188,574,873 GULP1
    nsv3879685copy number variation1nstd102humanBenign GRCh37 chr2: 189,122,229-189,330,900 , GRCh38.p12 chr2: 188,257,502-188,466,173 GULP1, MIR561, 2 more genes
    nsv3889556copy number variation1nstd102humanBenign GRCh37 chr2: 189,119,837-189,154,925 , GRCh38.p12 chr2: 188,255,110-188,290,198 GULP1, RNA5SP114, 1 more genes
    nsv3917182copy number variation1nstd102humanUncertain significance NCBI36 chr2: 188,615,798-189,056,210 , GRCh37.p13 chr2: 188,907,553-189,347,965 , GRCh38.p12 chr2: 188,042,826-188,483,238 GULP1, MIR561, 3 more genes
    nsv6291232copy number variation1nstd102humanUncertain significance GRCh37 chr2: 188,806,903-189,166,330 , GRCh38.p12 chr2: 187,942,176-188,301,603 GULP1, RNA5SP114, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 GULP1, DAZAP2P1, 2991 more genes
    nsv3894939copy number variation1nstd102humanPathogenic NCBI36 chr2: 175,471,822-204,514,516 , GRCh37 chr2: 175,763,576-204,806,271 , GRCh38 chr2: 174,898,848-203,941,548 GULP1, TRE-TTC9-1, 412 more genes
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 GULP1, LOC107985785, 381 more genes
    nsv3899404copy number variation1nstd102humanPathogenic NCBI36 chr2: 176,877,419-202,612,758 , GRCh37 chr2: 177,169,173-202,904,513 , GRCh38 chr2: 176,304,445-202,039,790 GULP1, LINC01877, 326 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 GULP1, LINC01117, 339 more genes
    nsv4674757copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858 GULP1, OSBPL6, 256 more genes
    nsv3895293copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,738,797-199,390,216 , NCBI36 chr2: 178,447,043-199,098,461 , GRCh38 chr2: 177,874,070-198,525,492 GULP1, CALCRL-AS1, 218 more genes
    nsv3878976copy number variation1nstd102humanPathogenic GRCh37 chr2: 177,315,153-196,375,520 , GRCh38.p12 chr2: 176,450,425-195,510,796 GULP1, FSIP2-AS1, 202 more genes
    nsv3891673copy number variation1nstd102humanPathogenic GRCh37 chr2: 172,285,743-190,044,294 , GRCh38 chr2: 171,429,233-189,179,568 , NCBI36 chr2: 171,993,989-189,752,539 GULP1, LOC729141, 238 more genes
    nsv3900193copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,692,457-195,990,053 , NCBI36 chr2: 178,400,703-195,698,298 , GRCh38 chr2: 177,827,730-195,125,329 GULP1, OSBPL6, 171 more genes
    nsv3905582copy number variation1nstd102humanPathogenic GRCh38 chr2: 176,086,763-193,201,970 , NCBI36 chr2: 176,659,737-193,774,941 , GRCh37 chr2: 176,951,491-194,066,696 GULP1, RPL23AP35, 211 more genes
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